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复发性胶质母细胞瘤切除术后辅助立体定向分次放疗 - GlioCave 研究(NOA 17 - ARO 2016/3 - DKTK ROG 试验)。

Adjuvant stereotactic fractionated radiotherapy to the resection cavity in recurrent glioblastoma - the GlioCave study (NOA 17 - ARO 2016/3 - DKTK ROG trial).

机构信息

Klinik für RadioOnkologie und Strahlentherapie, Technische Universität München (TUM), Ismaninger Straße 22, 81675, Munich, Germany.

Deutsches Konsortium für Translationale Krebsforschung (DKTK) - Partner Site Munich, 81675, Munich, Germany.

出版信息

BMC Cancer. 2018 Jan 3;18(1):15. doi: 10.1186/s12885-017-3928-7.

Abstract

BACKGROUND

Glioblastoma relapses in the vast majority of cases within 1 year. Maximum safe resection of the recurrent glioblastoma can be offered in some cases. Re-irradiation has been established for the treatment of recurrent glioblastoma, too. In both cases, adjuvant treatment, mostly using temozolomide, can improve PFS and OS after these interventions. However, combining gross tumor resection and adjuvant re-radiotherapy to the resection cavity has not been tested so far.

METHODS/DESIGN: In the multicenter two-armed randomized Phase II GlioCave Study, fractionated stereotactic radiotherapy to the resection cavity, after gross tumor resection of recurrent glioblastoma, will be compared to observation. Depending on the size of the target volume, a total dose of 46 Gy in 2 Gy per fraction or a total dose if 36 Gy in 3 Gy per fraction will be applied. Progression free survival will be the primary endpoint of the study.

DISCUSSION

Adjuvant treatment after gross tumor resection of recurrent glioblastoma is currently deemed to be limited to chemotherapy. However, re-irradiation has proven safety and tolerability in the treatment of macroscopic disease. Performing re-irradiation as an adjuvant measure after gross tumor resection has not been tested so far. The GlioCave Study will investigate the efficacy and the safety profile of this approach.

TRIAL REGISTRATION

The trial was prospectively registered at clinicaltrials.gov ( NCT02715297 , registration date February 29th, 2016). The protocol presented hereby refers to the version 1.2 of the protocol (January 11, 2017).

摘要

背景

绝大多数情况下,胶质母细胞瘤在 1 年内复发。在某些情况下,可以对复发性胶质母细胞瘤进行最大限度的安全切除。再放疗也已被确立为复发性胶质母细胞瘤的治疗方法。在这两种情况下,辅助治疗(通常使用替莫唑胺)可以改善这些干预措施后的无进展生存期和总生存期。然而,到目前为止,还没有测试过将大体肿瘤切除术和辅助再放疗联合应用于切除腔。

方法/设计:在多中心、双臂、随机、二期 GlioCave 研究中,在对复发性胶质母细胞瘤进行大体肿瘤切除后,对切除腔进行分次立体定向放疗,将与观察进行比较。根据靶区体积的大小,采用 2 Gy/次的 46 Gy 总剂量或 3 Gy/次的 36 Gy 总剂量进行治疗。无进展生存期将是该研究的主要终点。

讨论

复发性胶质母细胞瘤大体肿瘤切除后的辅助治疗目前被认为仅限于化疗。然而,再放疗在治疗宏观疾病方面已被证明是安全且耐受的。到目前为止,还没有测试过在大体肿瘤切除后将再放疗作为辅助措施进行。GlioCave 研究将调查这种方法的疗效和安全性。

试验注册

该试验在 clinicaltrials.gov 上进行了前瞻性注册(NCT02715297,注册日期为 2016 年 2 月 29 日)。本方案所指的是方案的 1.2 版本(2017 年 1 月 11 日)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f31/5753454/d35a590e9466/12885_2017_3928_Fig1_HTML.jpg

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